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Phelline comosa

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Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
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Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID644002369c559048685805
Scientific name Phelline comosa
Authority Labill.
First published in Sert. Austro-Caledon. : 35 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Phelline confertifolia Baill. Bull. Mens. Soc. Linn. Paris 2: 937 (1891)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000482185
Tropicos 50195873
INPN 674381
KEW urn:lsid:ipni.org:names:774765-1
Open Tree Of Life 593937
NCBI Taxonomy 4304
IUCN Red List 136828201
IPNI 83911-1
iNaturalist 943013
GBIF 4196454
EPPO QHECO
USDA GRIN 450551

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
New Homoerythrinane Alkaloids from Phelline Species Nicole Langlois The Japan Institute of Heterocyclic Chemistry 03-Mar-2009
doi:10.3987/COM-89-S91
Isophellibilidine, a new alkaloid of Phelline billiardieri: structure and hemisynthesis Nicole Langlois Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)92905-3
Homoerythrina alkaloids of Phelline comosa Adetunji J. Aladsesanmi, John K. Snyder, Charles J. Kelley, joseph J. Hoffmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83245-G
Alkaloids of Phelline comosa var. Robusta Jacques Pusset, Stephane La Barre, Nicole Langlois, Jeannine Hamon Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80243-2
East Gondwana ancestry of the sunflower alliance of families Bremer K, Gustafsson MH Proc Natl Acad Sci U S A 19-Aug-1997
PMCID:PMC23106
doi:10.1073/pnas.94.17.9188
PMID:9256457

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Erythrina alkaloids / Homoerythrinane alkaloids
(1R,13R,15S,18R)-4,18-dimethoxy-14-oxa-11-azapentacyclo[9.8.0.01,15.02,7.013,15]nonadeca-2,4,6,16-tetraen-5-ol 163007685 Click to see COC1CC23C4=CC(=C(C=C4CCCN2CC5C3(O5)C=C1)O)OC 329.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1R,13R,15S,18R)-5,18-dimethoxy-14-oxa-11-azapentacyclo[9.8.0.01,15.02,7.013,15]nonadeca-2,4,6,16-tetraen-4-ol 163073679 Click to see COC1CC23C4=CC(=C(C=C4CCCN2CC5C3(O5)C=C1)OC)O 329.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1R,14S,16R,18R)-4,5,6,18-tetramethoxy-15-oxa-11-azapentacyclo[9.8.0.01,14.02,7.014,16]nonadeca-2,4,6-triene 162908052 Click to see COC1CC2C3(O2)CCN4C3(C1)C5=CC(=C(C(=C5CCC4)OC)OC)OC 375.50 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1R,17S,19R,21R)-21-methoxy-5,7,18-trioxa-14-azahexacyclo[12.8.0.01,17.02,10.04,8.017,19]docosa-2,4(8),9-triene 163031072 Click to see COC1CC2C3(O2)CCN4C3(C1)C5=CC6=C(C=C5CCC4)OCO6 329.40 unknown https://doi.org/10.3987/COM-89-S91
(1R,17S,19R,21R)-5,7,18-trioxa-14-azahexacyclo[12.8.0.01,17.02,10.04,8.017,19]docosa-2,4(8),9-trien-21-ol 163044243 Click to see C1CC2=CC3=C(C=C2C45CC(CC6C4(O6)CCN5C1)O)OCO3 315.40 unknown https://doi.org/10.3987/COM-89-S91
(1S,14R,17R)-4,17-dimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,15-tetraen-5-ol 162904639 Click to see COC1CC23C(CCN2CCCC4=CC(=C(C=C34)OC)O)C=C1 315.40 unknown https://doi.org/10.3987/COM-89-S91
(1S,14R,17R)-5,17-dimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,15-tetraen-4-ol 14081840 Click to see COC1CC23C(CCN2CCCC4=CC(=C(C=C34)O)OC)C=C1 315.40 unknown https://doi.org/10.3987/COM-89-S91
(1S,14S,17R)-4,5,17-trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,15-tetraene 162959934 Click to see COC1CC23C(CCN2CCCC4=CC(=C(C=C34)OC)OC)C=C1 329.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1S,16S,17R)-4,5,17-trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-16-ol 163010767 Click to see COC1CC23C(=CC1O)CCN2CCCC4=CC(=C(C=C34)OC)OC 345.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1S,16S,17R)-4,5,6,17-tetramethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-16-ol 163019617 Click to see COC1CC23C(=CC1O)CCN2CCCC4=C(C(=C(C=C34)OC)OC)OC 375.50 unknown https://doi.org/10.1016/0031-9422(91)83245-G
(1S,17R,20R)-20-methoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,18-tetraene 15286562 Click to see COC1CC23C(CCN2CCCC4=CC5=C(C=C34)OCO5)C=C1 313.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1S,17S,20R)-20-methoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,18-tetraene 163186960 Click to see COC1CC23C(CCN2CCCC4=CC5=C(C=C34)OCO5)C=C1 313.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1S,17S)-4,5,6-trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-17-ol 162900686 Click to see COC1=C(C(=C2CCCN3CCC4=CCC(CC43C2=C1)O)OC)OC 345.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
https://doi.org/10.3987/COM-89-S91
(1S,17S)-4,5,6,17-tetramethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene 101690776 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)OC 359.50 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1S,17S)-5,6-dimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene-4,17-diol 163058139 Click to see COC1=C2CCCN3CCC4=CCC(CC43C2=CC(=C1OC)O)O 331.40 unknown https://doi.org/10.3987/COM-89-S91
(1S,17S)-5,6,17-trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-4-ol 101691087 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)O 345.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
(1S,19S,20R)-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraene-19,20-diol 162873489 Click to see C1CC2=CC3=C(C=C2C45CC(C(C=C4CCN5C1)O)O)OCO3 315.40 unknown https://doi.org/10.3987/COM-89-S91
(1S,19S,20R)-9,20-dimethoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraen-19-ol 162932111 Click to see COC1CC23C(=CC1O)CCN2CCCC4=C(C5=C(C=C34)OCO5)OC 359.40 unknown https://doi.org/10.1016/0031-9422(91)83245-G
20-Methoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,18-tetraene 102115609 Click to see COC1CC23C(CCN2CCCC4=CC5=C(C=C34)OCO5)C=C1 313.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
21-Methoxy-5,7,18-trioxa-14-azahexacyclo[12.8.0.01,17.02,10.04,8.017,19]docosa-2,4(8),9-triene 163031071 Click to see COC1CC2C3(O2)CCN4C3(C1)C5=CC6=C(C=C5CCC4)OCO6 329.40 unknown https://doi.org/10.3987/COM-89-S91
3-Epi-schelhammericine 296196 Click to see COC1CC=C2CCN3C2(C1)C4=CC5=C(C=C4CCC3)OCO5 313.40 unknown https://doi.org/10.1016/0031-9422(91)83245-G
3-Epiwilsonine 91895284 Click to see COC1CC23C4=CC(=C(C=C4CCCN2CC5C3(O5)C=C1)OC)OC 343.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
4,17-Dimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,15-tetraen-5-ol 14605246 Click to see COC1CC23C(CCN2CCCC4=CC(=C(C=C34)OC)O)C=C1 315.40 unknown https://doi.org/10.3987/COM-89-S91
4,18-Dimethoxy-14-oxa-11-azapentacyclo[9.8.0.01,15.02,7.013,15]nonadeca-2,4,6,16-tetraen-5-ol 14286118 Click to see COC1CC23C4=CC(=C(C=C4CCCN2CC5C3(O5)C=C1)O)OC 329.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
4,5,17-Trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-16-ol 5316553 Click to see COC1CC23C(=CC1O)CCN2CCCC4=CC(=C(C=C34)OC)OC 345.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
4,5,6-Trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-17-ol 14286112 Click to see COC1=C(C(=C2CCCN3CCC4=CCC(CC43C2=C1)O)OC)OC 345.40 unknown https://doi.org/10.3987/COM-89-S91
https://doi.org/10.1016/0031-9422(89)80243-2
4,5,6,17-Tetramethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-16-ol 163019616 Click to see COC1CC23C(=CC1O)CCN2CCCC4=C(C(=C(C=C34)OC)OC)OC 375.50 unknown https://doi.org/10.1016/0031-9422(91)83245-G
4,5,6,17-Tetramethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene 14286108 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)OC 359.50 unknown https://doi.org/10.1016/0031-9422(89)80243-2
4,5,6,18-Tetramethoxy-15-oxa-11-azapentacyclo[9.8.0.01,14.02,7.014,16]nonadeca-2,4,6-triene 14286114 Click to see COC1CC2C3(O2)CCN4C3(C1)C5=CC(=C(C(=C5CCC4)OC)OC)OC 375.50 unknown https://doi.org/10.1016/0031-9422(89)80243-2
5,17-Dimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,15-tetraen-4-ol 14081839 Click to see COC1CC23C(CCN2CCCC4=CC(=C(C=C34)O)OC)C=C1 315.40 unknown https://doi.org/10.3987/COM-89-S91
5,18-Dimethoxy-14-oxa-11-azapentacyclo[9.8.0.01,15.02,7.013,15]nonadeca-2,4,6,16-tetraen-4-ol 14286116 Click to see COC1CC23C4=CC(=C(C=C4CCCN2CC5C3(O5)C=C1)OC)O 329.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
5,6-Dimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraene-4,17-diol 14605242 Click to see COC1=C2CCCN3CCC4=CCC(CC43C2=CC(=C1OC)O)O 331.40 unknown https://doi.org/10.3987/COM-89-S91
5,6,17-Trimethoxy-11-azatetracyclo[9.7.0.01,14.02,7]octadeca-2,4,6,14-tetraen-4-ol 14286110 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=C(C(=C4CCC3)OC)OC)O 345.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
5,7-Dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraene-19,20-diol 14605244 Click to see C1CC2=CC3=C(C=C2C45CC(C(C=C4CCN5C1)O)O)OCO3 315.40 unknown https://doi.org/10.3987/COM-89-S91
5,7,18-Trioxa-14-azahexacyclo[12.8.0.01,17.02,10.04,8.017,19]docosa-2,4(8),9-trien-21-ol 163044242 Click to see C1CC2=CC3=C(C=C2C45CC(CC6C4(O6)CCN5C1)O)OCO3 315.40 unknown https://doi.org/10.3987/COM-89-S91
9,20-Dimethoxy-5,7-dioxa-14-azapentacyclo[12.7.0.01,17.02,10.04,8]henicosa-2,4(8),9,17-tetraen-19-ol 162932110 Click to see COC1CC23C(=CC1O)CCN2CCCC4=C(C5=C(C=C34)OCO5)OC 359.40 unknown https://doi.org/10.1016/0031-9422(91)83245-G
Alkaloid PC-II 14081836 Click to see COC1CC23C(CCN2CCCC4=CC(=C(C=C34)OC)OC)C=C1 329.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
Wilsonine 630102 Click to see COC1CC23C4=CC(=C(C=C4CCCN2CC5C3(O5)C=C1)OC)OC 343.40 unknown https://doi.org/10.1016/0031-9422(89)80243-2
> Alkaloids and derivatives / Stemona alkaloids / Stemoamide-type alkaloids
(1S,6S,16S)-6-(hydroxymethyl)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,6]heptadeca-2,13-dien-4-one 101592486 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=O)OC4(CCC3)CO 305.40 unknown https://doi.org/10.1016/S0040-4039(01)92905-3
6-(Hydroxymethyl)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,6]heptadeca-2,13-dien-4-one 163014191 Click to see COC1CC=C2CCN3C2(C1)C4=CC(=O)OC4(CCC3)CO 305.40 unknown https://doi.org/10.1016/S0040-4039(01)92905-3

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